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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1430804생성일: 2026년 10월 25일

Lithium Hexamethyldisilazide → 7-bromo-N-cyclopropyl-N-(4-methoxybenzyl)-2-(methylthio)imidazo[2,1-f][1,2,4]triazin-4-amine

https://huagongshe.com/reaction/1430804

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물N-((4-methoxyphenyl)methyl)cyclopropanamineHCID 4721289—
반응물7-Bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazineHCID 57457644—
용매TetrahydrofuranHCID 8028—
생성물7-bromo-N-cyclopropyl-N-(4-methoxybenzyl)-2-(methylthio)imidazo[2,1-f][1,2,4]triazin-4-amineHCID 8670849072.7%

반응 조건

온도-78 °C

반응 단계

To a 25 mL flask was added a mixture of 7-bromo-2,4-bis(methylthio)imidazo[2,1-f][1,2,4]triazine (2.0 g, 6.87 mmol), N-(4-methoxybenzyl)cyclopropanamine (1.34 g, 7.56 mmol) in anhydrous THF (20 mL). The reaction solution was cooled to −78° C. and treated dropwise with 1.0 M lithium bis(trimethylsilyl)amide in THF solution (20.61 mL, 20.61 mmol, 3 eq, 1M solution in THF). The reaction was stirred at −78° C. for 1 hour, then allowed to come to room temperature and stirred for 3 hours The reaction was quenched with saturated ammonium chloride. The product was extracted with ethyl acetate, the organic layer was dried with sodium sulfate and concentrated in vacuo. The crude product mixture was purified via ISCO (0-100% of ethyl acetate/heptane in 10 minutes, 24 g silica column) to give the pure product 7-bromo-N-cyclopropyl-N-(4-methoxybenzyl)-2-(methylthio)imidazo[2,1-f][1,2,4]triazin-4-amine (2.1 g)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08940736B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-7a1a5621a2574bd2ba679a66047b6b06
출처 메모uspto-grants-2015_01